Does PIRFENIDONE Cause Product dose omission in error? 159 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 159 reports of Product dose omission in error have been filed in association with PIRFENIDONE (PIRFENIDONE). This represents 0.4% of all adverse event reports for PIRFENIDONE.
159
Reports of Product dose omission in error with PIRFENIDONE
0.4%
of all PIRFENIDONE reports
1
Deaths
10
Hospitalizations
How Dangerous Is Product dose omission in error From PIRFENIDONE?
Of the 159 reports, 1 (0.6%) resulted in death, 10 (6.3%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PIRFENIDONE. However, 159 reports have been filed with the FAERS database.
What Other Side Effects Does PIRFENIDONE Cause?
Death (7,221)
Nausea (4,944)
Fatigue (3,597)
Decreased appetite (3,126)
Diarrhoea (3,026)
Dyspnoea (2,526)
Weight decreased (2,113)
Dizziness (2,027)
Rash (1,982)
Cough (1,692)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which PIRFENIDONE Alternatives Have Lower Product dose omission in error Risk?
PIRFENIDONE vs PIRIBEDIL
PIRFENIDONE vs PIRITRAMIDE
PIRFENIDONE vs PIROXICAM
PIRFENIDONE vs PIRTOBRUTINIB
PIRFENIDONE vs PIT VIPER IMMUNE GLOBULIN ANTIVENIN